ADVANCED SURGICAL PRODUCTS SCLERAL PLUG FORCEPS— 510(k) K880274

Name: FDA 510(k) clearance K880274
Creator: U.S. Food and Drug Administration
Published: 1988-02-05

Substantially Equivalent

Advanced Surgical Products, Inc.

FDA 510(k) clearance K880274 for ADVANCED SURGICAL PRODUCTS SCLERAL PLUG FORCEPS, Substantially Equivalent on 1988-02-05. Applicant: Advanced Surgical Products, Inc.. Device class: 1.

Clearance details

Applicant: Advanced Surgical Products, Inc.
Product code: Code HNR
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1988-01-21
Decision date: 1988-02-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chesterfield, MO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HNR

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K022835 — STEPHENS DISPOSABLE FORCEPS2002-11-01
K895434 — ALCON FOLDING FORCEPS1989-12-04
K891487 — SOFT LENS FOLDING BLOCK1989-08-15
K893199 — PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTR1989-06-16
K885230 — MCDONALD FOLDING FORCEPS1989-05-17

More clearances from Advanced Surgical Products, Inc.

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K030926 — FAST THROW STAINLESS STEEL SURGICAL SUTURE2003-07-21
K895800 — ADVANCED SURGICAL SOLID STATE BIPOLAR COAGULATOR1990-01-22
K896754 — I/A HANDPIECE1990-01-11
K896305 — MULTI-USE I/A HANDPIECE1989-12-18
K884557 — ADVANCED SURGICAL PRODUCTS SCISSORS HANDPIECE1989-05-12

Adverse events under product code HNR

product code HNR

Malfunction: 497
Other: 1
Total: 498

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.